Molecules

Name	Type	Specific against	Appl.	Item no.	Amount	Price
MUN36378	Chemicals	Other		DCC-DC60107-100mg DCChemicals	100 mg	Login Compare	MUN36378
MUN36378	Chemicals	Other		DCC-DC60107-250mg DCChemicals	250 mg	Login Compare	MUN36378
MUN36378	Chemicals	Other		DCC-DC60107-1g DCChemicals	1 g	Login Compare	MUN36378
AZ-7550 Mesylate	Chemicals	Other	AZ7550 Mesylate is an active metabolite of AZD9291 (Osimertinib) and inhibits the activity of IGF1R with an IC50 of 1.6 μM.	DCC-DC60108-10mg DCChemicals	10 mg	Login Compare	AZ-7550 Mesylate
Brevifolincarboxylic acid	Chemicals	Other	Brevifolincarboxylic acid is extracted from Polygonum capitatum, has inhibitory effect on the aryl hydrocarbon receptor (AhR). Brevifolincarboxylic acid has anticancer and anti-inflammatory activities	DCC-DC60109-10mg DCChemicals	10 mg	Login Compare	Brevifolincarboxylic acid
Pimethixene	Chemicals	Other	Pimethixene or Calmixen is antihistamine and anticholinergic of the thioxanthene chemical class that is often used to treat hyperactivity, anxiety, sleep disorders, and allergy.	DCC-DC60116-100mg DCChemicals	100 mg	Login Compare	Pimethixene
Pimethixene	Chemicals	Other	Pimethixene or Calmixen is antihistamine and anticholinergic of the thioxanthene chemical class that is often used to treat hyperactivity, anxiety, sleep disorders, and allergy.	DCC-DC60116-250mg DCChemicals	250 mg	Login Compare	Pimethixene
Pimethixene	Chemicals	Other	Pimethixene or Calmixen is antihistamine and anticholinergic of the thioxanthene chemical class that is often used to treat hyperactivity, anxiety, sleep disorders, and allergy.	DCC-DC60116-1g DCChemicals	1 g	Login Compare	Pimethixene
RS-25344 hydrochloride	Chemicals	Other	RS-25344 HCl is a potent and selective phosphodiesterase (PDE) 4 inhibitor (IC50 values are 0.28, > 100, 160 and 330 nM at PDE4, PDE1, PDE2 and PDE3 respectively). It inhibits eosinophil chemotaxis and increases progressive motility of spermatozoa in vitro.	DCC-DC60117-100mg DCChemicals	100 mg	Login Compare	RS-25344 hydrochloride
RS-25344 hydrochloride	Chemicals	Other	RS-25344 HCl is a potent and selective phosphodiesterase (PDE) 4 inhibitor (IC50 values are 0.28, > 100, 160 and 330 nM at PDE4, PDE1, PDE2 and PDE3 respectively). It inhibits eosinophil chemotaxis and increases progressive motility of spermatozoa in vitro.	DCC-DC60117-250mg DCChemicals	250 mg	Login Compare	RS-25344 hydrochloride
RS-25344 hydrochloride	Chemicals	Other	RS-25344 HCl is a potent and selective phosphodiesterase (PDE) 4 inhibitor (IC50 values are 0.28, > 100, 160 and 330 nM at PDE4, PDE1, PDE2 and PDE3 respectively). It inhibits eosinophil chemotaxis and increases progressive motility of spermatozoa in vitro.	DCC-DC60117-1g DCChemicals	1 g	Login Compare	RS-25344 hydrochloride
QQN05022(Dot1L-IN-4)	Chemicals	Other	Dot	DCC-DC60120-100mg DCChemicals	100 mg	Login Compare	QQN05022(Dot1L-IN-4)
QQN05022(Dot1L-IN-4)	Chemicals	Other	Dot	DCC-DC60120-250mg DCChemicals	250 mg	Login Compare	QQN05022(Dot1L-IN-4)
QQN05022(Dot1L-IN-4)	Chemicals	Other	Dot	DCC-DC60120-1g DCChemicals	1 g	Login Compare	QQN05022(Dot1L-IN-4)
N-desethyl Amodiaquine HCl	Chemicals	Other	N-desethyl Amodiaquine is a primary metabolite of the antimalarial compound aminodiaquine, produced by the action of cytochrome P450 isoform 2C8. N-desethyl Amodiaquine is highly active against P. falciparum and can synergize with amodiaquine.	DCC-DC60123-100mg DCChemicals	100 mg	Login Compare	N-desethyl Amodiaquine HCl
N-desethyl Amodiaquine HCl	Chemicals	Other	N-desethyl Amodiaquine is a primary metabolite of the antimalarial compound aminodiaquine, produced by the action of cytochrome P450 isoform 2C8. N-desethyl Amodiaquine is highly active against P. falciparum and can synergize with amodiaquine.	DCC-DC60123-250mg DCChemicals	250 mg	Login Compare	N-desethyl Amodiaquine HCl
N-desethyl Amodiaquine HCl	Chemicals	Other	N-desethyl Amodiaquine is a primary metabolite of the antimalarial compound aminodiaquine, produced by the action of cytochrome P450 isoform 2C8. N-desethyl Amodiaquine is highly active against P. falciparum and can synergize with amodiaquine.	DCC-DC60123-1g DCChemicals	1 g	Login Compare	N-desethyl Amodiaquine HCl
IL-1R antagonist(TLR1)	Chemicals	Other	IL-1R antagonist, is a peptide mimic of the myeloid differentiation primary response gene 88 (MyD88) that changes the interaction of MyD88 and IL-1 receptor type I (IL-1RI). This product has not formal name.	DCC-DC60081-100mg DCChemicals	100 mg	Login Compare	IL-1R antagonist(TLR1)
IL-1R antagonist(TLR1)	Chemicals	Other	IL-1R antagonist, is a peptide mimic of the myeloid differentiation primary response gene 88 (MyD88) that changes the interaction of MyD88 and IL-1 receptor type I (IL-1RI). This product has not formal name.	DCC-DC60081-250mg DCChemicals	250 mg	Login Compare	IL-1R antagonist(TLR1)
IL-1R antagonist(TLR1)	Chemicals	Other	IL-1R antagonist, is a peptide mimic of the myeloid differentiation primary response gene 88 (MyD88) that changes the interaction of MyD88 and IL-1 receptor type I (IL-1RI). This product has not formal name.	DCC-DC60081-1g DCChemicals	1 g	Login Compare	IL-1R antagonist(TLR1)
5-ethyl-4-methyl-N-{4-[(2S)-morpholin-2-yl]phenyl}-1Hpyrazole-3-carboxamide hydrochloride	Chemicals	Other	Ralmitaront, also known as WHO 11130, RO 6889450 and RG7906, is a neuroleptic.	DCC-DC60049-100mg DCChemicals	100 mg	Login Compare	5-ethyl-4-methyl-N-{4-[(2S)-morpholin-2-yl]phenyl}-1Hpyrazole-3-carboxamide hydrochloride
5-ethyl-4-methyl-N-{4-[(2S)-morpholin-2-yl]phenyl}-1Hpyrazole-3-carboxamide hydrochloride	Chemicals	Other	Ralmitaront, also known as WHO 11130, RO 6889450 and RG7906, is a neuroleptic.	DCC-DC60049-250mg DCChemicals	250 mg	Login Compare	5-ethyl-4-methyl-N-{4-[(2S)-morpholin-2-yl]phenyl}-1Hpyrazole-3-carboxamide hydrochloride
5-ethyl-4-methyl-N-{4-[(2S)-morpholin-2-yl]phenyl}-1Hpyrazole-3-carboxamide hydrochloride	Chemicals	Other	Ralmitaront, also known as WHO 11130, RO 6889450 and RG7906, is a neuroleptic.	DCC-DC60049-1g DCChemicals	1 g	Login Compare	5-ethyl-4-methyl-N-{4-[(2S)-morpholin-2-yl]phenyl}-1Hpyrazole-3-carboxamide hydrochloride
JH-X-119-01	Chemicals	Other	Jh-X-119-01 is a novel potent and selective interleukin-1 receptor-associated kinases 1 (IRAK1) inhibitor. JH-X-119-01 irreversibly labels IRAK1 at C302. This compound exhibited cytotoxic activity at single digit micromolar concentrations in a panel of WM, DLBCL, and lymphoma cell lines expressing MYD88. Cotreatment of JH-X-119-01 with the BTK inhibitor ibrutinib resulted in synergistic killing effects in these systems.	DCC-DC60125-100mg DCChemicals	100 mg	Login Compare	JH-X-119-01
JH-X-119-01	Chemicals	Other	Jh-X-119-01 is a novel potent and selective interleukin-1 receptor-associated kinases 1 (IRAK1) inhibitor. JH-X-119-01 irreversibly labels IRAK1 at C302. This compound exhibited cytotoxic activity at single digit micromolar concentrations in a panel of WM, DLBCL, and lymphoma cell lines expressing MYD88. Cotreatment of JH-X-119-01 with the BTK inhibitor ibrutinib resulted in synergistic killing effects in these systems.	DCC-DC60125-250mg DCChemicals	250 mg	Login Compare	JH-X-119-01

Name Price

MUN36378

Type	Chemicals
Clone
Specific against	Other
Appl.
Host
Item no.	DCC-DC60107-100mg
Amount	100 mg
Available

MUN36378

Type	Chemicals
Clone
Specific against	Other
Appl.
Host
Item no.	DCC-DC60107-250mg
Amount	250 mg
Available

MUN36378

Type	Chemicals
Clone
Specific against	Other
Appl.
Host
Item no.	DCC-DC60107-1g
Amount	1 g
Available

AZ-7550 Mesylate

Type	Chemicals
Clone
Specific against	Other
Appl.	AZ7550 Mesylate is an active metabolite of AZD9291 (Osimertinib) and inhibits the activity of IGF1R with an IC50 of 1.6 μM.
Host
Item no.	DCC-DC60108-10mg
Amount	10 mg
Available

Brevifolincarboxylic acid

Type	Chemicals
Clone
Specific against	Other
Appl.	Brevifolincarboxylic acid is extracted from Polygonum capitatum, has inhibitory effect on the aryl hydrocarbon receptor (AhR). Brevifolincarboxylic acid has anticancer and anti-inflammatory activities
Host
Item no.	DCC-DC60109-10mg
Amount	10 mg
Available

Pimethixene

Type	Chemicals
Clone
Specific against	Other
Appl.	Pimethixene or Calmixen is antihistamine and anticholinergic of the thioxanthene chemical class that is often used to treat hyperactivity, anxiety, sleep disorders, and allergy.
Host
Item no.	DCC-DC60116-100mg
Amount	100 mg
Available

Pimethixene

Type	Chemicals
Clone
Specific against	Other
Appl.	Pimethixene or Calmixen is antihistamine and anticholinergic of the thioxanthene chemical class that is often used to treat hyperactivity, anxiety, sleep disorders, and allergy.
Host
Item no.	DCC-DC60116-250mg
Amount	250 mg
Available

Pimethixene

Type	Chemicals
Clone
Specific against	Other
Appl.	Pimethixene or Calmixen is antihistamine and anticholinergic of the thioxanthene chemical class that is often used to treat hyperactivity, anxiety, sleep disorders, and allergy.
Host
Item no.	DCC-DC60116-1g
Amount	1 g
Available

RS-25344 hydrochloride

Type	Chemicals
Clone
Specific against	Other
Appl.	RS-25344 HCl is a potent and selective phosphodiesterase (PDE) 4 inhibitor (IC50 values are 0.28, > 100, 160 and 330 nM at PDE4, PDE1, PDE2 and PDE3 respectively). It inhibits eosinophil chemotaxis and increases progressive motility of spermatozoa in vitro.
Host
Item no.	DCC-DC60117-100mg
Amount	100 mg
Available

RS-25344 hydrochloride

Type	Chemicals
Clone
Specific against	Other
Appl.	RS-25344 HCl is a potent and selective phosphodiesterase (PDE) 4 inhibitor (IC50 values are 0.28, > 100, 160 and 330 nM at PDE4, PDE1, PDE2 and PDE3 respectively). It inhibits eosinophil chemotaxis and increases progressive motility of spermatozoa in vitro.
Host
Item no.	DCC-DC60117-250mg
Amount	250 mg
Available

RS-25344 hydrochloride

Type	Chemicals
Clone
Specific against	Other
Appl.	RS-25344 HCl is a potent and selective phosphodiesterase (PDE) 4 inhibitor (IC50 values are 0.28, > 100, 160 and 330 nM at PDE4, PDE1, PDE2 and PDE3 respectively). It inhibits eosinophil chemotaxis and increases progressive motility of spermatozoa in vitro.
Host
Item no.	DCC-DC60117-1g
Amount	1 g
Available

QQN05022(Dot1L-IN-4)

Type	Chemicals
Clone
Specific against	Other
Appl.	Dot
Host
Item no.	DCC-DC60120-100mg
Amount	100 mg
Available

QQN05022(Dot1L-IN-4)

Type	Chemicals
Clone
Specific against	Other
Appl.	Dot
Host
Item no.	DCC-DC60120-250mg
Amount	250 mg
Available

QQN05022(Dot1L-IN-4)

Type	Chemicals
Clone
Specific against	Other
Appl.	Dot
Host
Item no.	DCC-DC60120-1g
Amount	1 g
Available

N-desethyl Amodiaquine HCl

Type	Chemicals
Clone
Specific against	Other
Appl.	N-desethyl Amodiaquine is a primary metabolite of the antimalarial compound aminodiaquine, produced by the action of cytochrome P450 isoform 2C8. N-desethyl Amodiaquine is highly active against P. falciparum and can synergize with amodiaquine.
Host
Item no.	DCC-DC60123-100mg
Amount	100 mg
Available

N-desethyl Amodiaquine HCl

Type	Chemicals
Clone
Specific against	Other
Appl.	N-desethyl Amodiaquine is a primary metabolite of the antimalarial compound aminodiaquine, produced by the action of cytochrome P450 isoform 2C8. N-desethyl Amodiaquine is highly active against P. falciparum and can synergize with amodiaquine.
Host
Item no.	DCC-DC60123-250mg
Amount	250 mg
Available

N-desethyl Amodiaquine HCl

Type	Chemicals
Clone
Specific against	Other
Appl.	N-desethyl Amodiaquine is a primary metabolite of the antimalarial compound aminodiaquine, produced by the action of cytochrome P450 isoform 2C8. N-desethyl Amodiaquine is highly active against P. falciparum and can synergize with amodiaquine.
Host
Item no.	DCC-DC60123-1g
Amount	1 g
Available

IL-1R antagonist(TLR1)

Type	Chemicals
Clone
Specific against	Other
Appl.	IL-1R antagonist, is a peptide mimic of the myeloid differentiation primary response gene 88 (MyD88) that changes the interaction of MyD88 and IL-1 receptor type I (IL-1RI). This product has not formal name.
Host
Item no.	DCC-DC60081-100mg
Amount	100 mg
Available

IL-1R antagonist(TLR1)

Type	Chemicals
Clone
Specific against	Other
Appl.	IL-1R antagonist, is a peptide mimic of the myeloid differentiation primary response gene 88 (MyD88) that changes the interaction of MyD88 and IL-1 receptor type I (IL-1RI). This product has not formal name.
Host
Item no.	DCC-DC60081-250mg
Amount	250 mg
Available

IL-1R antagonist(TLR1)

Type	Chemicals
Clone
Specific against	Other
Appl.	IL-1R antagonist, is a peptide mimic of the myeloid differentiation primary response gene 88 (MyD88) that changes the interaction of MyD88 and IL-1 receptor type I (IL-1RI). This product has not formal name.
Host
Item no.	DCC-DC60081-1g
Amount	1 g
Available

5-ethyl-4-methyl-N-{4-[(2S)-morpholin-2-yl]phenyl}-1Hpyrazole-3-carboxamide hydrochloride

Type	Chemicals
Clone
Specific against	Other
Appl.	Ralmitaront, also known as WHO 11130, RO 6889450 and RG7906, is a neuroleptic.
Host
Item no.	DCC-DC60049-100mg
Amount	100 mg
Available

5-ethyl-4-methyl-N-{4-[(2S)-morpholin-2-yl]phenyl}-1Hpyrazole-3-carboxamide hydrochloride

Type	Chemicals
Clone
Specific against	Other
Appl.	Ralmitaront, also known as WHO 11130, RO 6889450 and RG7906, is a neuroleptic.
Host
Item no.	DCC-DC60049-250mg
Amount	250 mg
Available

5-ethyl-4-methyl-N-{4-[(2S)-morpholin-2-yl]phenyl}-1Hpyrazole-3-carboxamide hydrochloride

Type	Chemicals
Clone
Specific against	Other
Appl.	Ralmitaront, also known as WHO 11130, RO 6889450 and RG7906, is a neuroleptic.
Host
Item no.	DCC-DC60049-1g
Amount	1 g
Available

JH-X-119-01

Type	Chemicals
Clone
Specific against	Other
Appl.	Jh-X-119-01 is a novel potent and selective interleukin-1 receptor-associated kinases 1 (IRAK1) inhibitor. JH-X-119-01 irreversibly labels IRAK1 at C302. This compound exhibited cytotoxic activity at single digit micromolar concentrations in a panel of WM, DLBCL, and lymphoma cell lines expressing MYD88. Cotreatment of JH-X-119-01 with the BTK inhibitor ibrutinib resulted in synergistic killing effects in these systems.
Host
Item no.	DCC-DC60125-100mg
Amount	100 mg
Available

JH-X-119-01

Type	Chemicals
Clone
Specific against	Other
Appl.	Jh-X-119-01 is a novel potent and selective interleukin-1 receptor-associated kinases 1 (IRAK1) inhibitor. JH-X-119-01 irreversibly labels IRAK1 at C302. This compound exhibited cytotoxic activity at single digit micromolar concentrations in a panel of WM, DLBCL, and lymphoma cell lines expressing MYD88. Cotreatment of JH-X-119-01 with the BTK inhibitor ibrutinib resulted in synergistic killing effects in these systems.
Host
Item no.	DCC-DC60125-250mg
Amount	250 mg
Available

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